Role Description The primary responsibility of the Clinical Research Associate I (CRA I) is support of the research team in the conduct of department research projects. - Perform study startup, implementation, and closeout activities - Assist research team with coordination and entry of research data - Assist with regulatory submissions to the Institutional Review Board, and maintain compliance with all federal and local agencies in accordance with Good Clinical Practice guidelines - Interact with patients and families for securing informed consent, scheduling research visits, and collection of data - Maintain documentation for regulatory binder, adverse event reporting, and communications between sponsors and sites - Other special skills specific to assigned research area may include phlebotomy, sample collection, processing or shipping, ECGs, chart abstraction or other duties as assigned - Manage personal career development and administrative tasks Qualifications - Baccalaureate degree or at least 4 years relevant clinical research, professional experience - High attention to detail with strong written and oral communication skills - Strong computer skills beyond basic familiarity with the most common hardware and software systems - Ability to assist staff working on multiple projects - Experience working with pediatric populations (preferred) Requirements Promotion to next higher level, typically CRA II, is determined by the Clinical Research Program Manager through performance reviews that take into account both experience carrying out the department's job-related duties/tasks, as well as a demonstrated commitment to professionalism in carrying out those tasks in line with Children's values and organizational policies and procedures. Benefits - Medical, dental, vision, retirement, and other fringe benefits - Positions that require night, weekend or on-call work may be eligible for shift differentials or premium pay

Role Description The Wilson Center invites scholars, practitioners, journalists, and public intellectuals to apply for its flagship Research Fellowship competition. Research Fellows conduct research and write in their areas of interest, while interacting with policymakers in Washington D.C. and with other Wilson Center fellows and staff. The Center accepts policy-relevant, nonpartisan fellowship proposals that address key challenges confronting the United States and the world. The focus of each fellow’s tenure will be their research project, which must meet the following criteria: - Projects must be nonpartisan in nature. - Projects must focus on at least one of the following scholarship pillars of the Wilson Center: - strategic competition - economic statecraft - technology and innovation - regional scholarship - Primary project outputs may include: - a book manuscript - a series of long-form articles - a briefing roundtable series for policymakers - Primary project outputs may not include: - rewriting or completion of doctoral dissertations - projects in the visual arts, dance, or musical composition - editing of texts, papers, and documents - preparations of textbooks, anthologies, translations, or memoirs In addition to their research project, fellows will be expected to actively contribute to the goals and mission of the Wilson Center during their tenure. The Center will work with all fellows to share their expertise with the Washington policy community, which may include: - deep background briefings for federal agencies - informal roundtable discussions with members of Congress and their staffs - formal presentations to the public such as colloquiums, seminars, workshops, or other meetings Fellows will also be encouraged to produce policy reports, op-eds, and other short written products during their tenure and engage with the broader Washington community of scholars working on similar topics. The Center will provide guidance for all fellows on translating academic research into policy-relevant content. Fellows will work remotely during their tenure with the Wilson Center, which includes a trip to Washington D.C. at the start and end of the fellowship, paid for by the Wilson Center. The fellowship will commence on June 1, 2027, and end on May 30, 2028. The Center offers a stipend of $10,000 per month for a twelve-month fellowship. Qualifications - Applicants from academia must have a PhD and have published a book or monograph beyond the PhD dissertation, or a substantial body of research articles (typically five or more) in reputable peer-reviewed journals. - Applicants from government, policy, or the nonprofit sector must have achieved a level of professional distinction and experience equivalent to advanced academic standing, typically at least 10 years of relevant experience and a record of substantial policy impact, publication, or leadership in their field. - Applicants must be proficient in English, as the Center is designed to encourage the exchange of ideas among its fellows and provide educational opportunities to Congress. - Applicants must be able to attend a fellowship kick-off meeting in June 2027 and a fellowship conclusion meeting in May 2028, both held at the Wilson Center in Washington D.C. - If resident in the United States, applicants must be U.S. citizens or legal permanent residents, as the Wilson Center is not able to sponsor J-1 visas. If the applicant intends to reside outside of the United States during the fellowship duration, they must hold a valid passport and be able to obtain the appropriate visa to travel to the United States. - No institutional affiliation is required to apply. Fellows may take leave from their current positions or maintain additional affiliations during their Wilson Center Research Fellowship.

• Completes daily reviews of all patient video submissions when ingesting medications, and responds as appropriate per engagement and escalation protocols, and documents actions taken • Updates and maintains a database of patient-level notes daily • Conducts data entry, data quality check, and data reconciliation exercises to ensure consistent documentation • Conducts technical training with study sites to help patients use Scene Health’s mobile application and to resolve technical challenges when using the web platform • Prepares written reports and maintains records of program monitoring activities • Works collaboratively with a cross-functional team to identify, develop, evaluate, and refine new processes and features of the Scene Health program • Provides management with patient feedback and/or recommendations for program and product improvement • Other duties as assigned

• Responsible for the timely and accurate preparation and maintenance of budgets for sponsored clinical trials • Review of New Study routing forms and essential study start-up documents • Itemized cost analysis and interpretation of clinical protocols into budget milestones • Provide accurate patient cost descriptions for the ICF to be submitted to the IRB • Update budget, milestones, and ICF information as necessary per contract/protocol amendments • Work closely with contract analysts, regulatory team, program managers and internal finance groups • Manage large volume workflow across multiple research programs • Develop study budgets from clinical studies protocols • Complete full evaluation and integration of internal cost during set-up of a new clinical study • Revise study budgets following revision of study protocols or re-assessment of study cost